ライフサイエンスコーパス: piriform cortex

1 t power gradient originating in the adjacent piriform cortex.

2 undant axo-axonic synapses across the entire piriform cortex.

3 operties of these synapses across the entire piriform cortex.

4 in putative centrifugal cells and posterior piriform cortex.

5 al migration and homologous to the mammalian piriform cortex.

6 sentations of odor identity and intensity in piriform cortex.

7 on of odors more similar to that seen in the piriform cortex.

8 y bulbs and higher brain regions such as the piriform cortex.

9 he lateral olfactory tract and the posterior piriform cortex.

10 al glutamatergic neurons within normal adult piriform cortex.

11 iate into pyramidal glutamatergic neurons in piriform cortex.

12 n local field potentials within the anterior piriform cortex.

13 integration and analogous to the vertebrate piriform cortex.

14 ctions with both the olfactory bulb (OB) and piriform cortex.

15 temporal cortices, with no changes noted in piriform cortex.

16 anatomical- and theoretical-based models of piriform cortex.

17 f the pseudorabies virus into the rat OB and piriform cortex.

18 y nucleus, the endopiriform nucleus, and the piriform cortex.

19 ctively expressed in different layers of the piriform cortex.

20 ating odor response properties of neurons in piriform cortex.

21 presentations of odor objects are encoded in piriform cortex.

22 principal excitatory neuron in the anterior piriform cortex.

23 tion of the intracortical axons in slices of piriform cortex.

24 ck end labeling [TUNEL]) in the rat anterior piriform cortex.

25 /median eminence, paraventricular nuclei and piriform cortex.

26 rs are initially encoded as 'objects' in the piriform cortex.

27 cell layer, thalamic reticular nucleus, and piriform cortex.

28 ost of which send strong projections back to piriform cortex.

29 tral/tufted (MT) cells carrying OB output to piriform cortex.

30 egions, including the supraoptic nucleus and piriform cortex.

31 roup of multipolar cells located deep to the piriform cortex.

32 t but not the associational afferents of the piriform cortex.

33 ives rich glutamatergic projections from the piriform cortex.

34 odel of cholinergic modulation in the OB and piriform cortex.

35 olfactory tract (lot) guidepost cells in the piriform cortex.

36 maker circuits in the septal nucleus and the piriform cortex.

37 b and in the pyramidal cells of the anterior piriform cortex.

38 ns, and later to layer II/III neurons of the piriform cortex.

39 olinergic modulation of the OB inputs to the piriform cortex.

40 ompared to juvenile rats in both the OFC and piriform cortex.

41 rom several areas, including S1, SR, FM, and piriform cortex.

42 bilateral reversible lesions of the anterior piriform cortex.

43 i.e., the hippocampus, substantia nigra, and piriform cortex.

44 ive input times than neurons in the anterior piriform cortex.

45 (mitral/tufted [MT] cells) projecting to the piriform cortex.

46 distributed in the rodent primary olfactory (piriform) cortex.

47 or representations in rat primary olfactory (piriform) cortex.

48 mble activity patterns in primary olfactory (piriform) cortex.

49 d are highly expressed in primary olfactory (piriform) cortex.

50 ity in the mouse primary olfactory (anterior piriform) cortex.

51 essing center for olfactory information, the piriform cortex?

52 L labeling in layers I/II of the ipsilateral piriform cortex 24 h after bulbectomy.

53 ippocampus=93%, neocortex=80-84%, entorhinal-piriform cortex=42%, amygdala=28%).

54 s involved the dorsal hippocampus (75%), the piriform cortex (87.5%), and the amygdala (25%).

55 The analysis was of piriform cortex, a highly epileptogenic area of cerebral

56 obust interhemispheric asymmetry in anterior piriform cortex activity that emerges during specific st

57 nput from the anterior olfactory nucleus and piriform cortex already by the second week.

58 Pyramidal cells in adult piriform cortex also lack I(h), the mixed Na(+)-K(+) cur

59 Labeled fibers in posterior piriform cortex also were seen after injection into orbi

60 We did not observe these effects in anterior piriform cortex, amygdala or orbitofrontal cortex, indic

61 t of local field potential activity in human piriform cortex, amygdala, and hippocampus.

62 xpressed in the olfactory bulb, hippocampus, piriform cortex, amygdala, hypothalamus, cerebellum, and

63 c-Jun immunoreactivity were observed in the piriform cortex, an area that also showed more positive

64 c suppression of responses from the amygdalo-piriform cortex, an associative temporal cortical struct

65 The three-layered piriform cortex, an integral part of the olfactory syste

66 Because these D1CT mice express CT in the piriform cortex and amygdala (major cognitive and affect

67 of the basal telencephalon, most notably the piriform cortex and amygdala.

68 cross brain regions, and particularly in the piriform cortex and cortical amygdala.

69 necrosis in susceptible brain regions (e.g., piriform cortex and hippocampal CA1 and CA3 regions).

70 dus within 3 h after KA treatment and in the piriform cortex and hippocampus by 6 h after KA.

71 reased theta-specific phase coupling between piriform cortex and hippocampus.

72 poxia on KA-induced edema attenuation in the piriform cortex and hippocampus.

73 us (AON) lies between the olfactory bulb and piriform cortex and is the first bilaterally innervated

74 d with a direct monosynaptic pathway linking piriform cortex and OFC.

75 Labeled fibers were found in the piriform cortex and olfactory bulb on the side ipsilater

76 , subsets of cells that populate the ventral piriform cortex and olfactory bulb reach these sites by

77 However, the LEC also projects back to the piriform cortex and olfactory bulb.

78 ible changes in odor-evoked fMRI activity in piriform cortex and orbitofrontal cortex (OFC).

79 ed by learning-induced response increases in piriform cortex and orbitofrontal cortex (OFC).

80 nfection from the olfactory bulb (OB) to the piriform cortex and other areas connected to the OB was

81 wever, it did not affect degeneration in the piriform cortex and PLCo indicating that limbic degenera

82 eurons in the somatosensory parietal cortex, piriform cortex and posterolateral cortical amygdaloid n

83 ns that resembled neurogliaform cells of the piriform cortex and provided feedforward inhibition of t

84 phe magnus nucleus, and was decreased in the piriform cortex and septum.

85 e, only C. sociabilis had OTR binding in the piriform cortex and thalamus and V1aR binding in the olf

86 idual glomeruli in the olfactory bulb to the piriform cortex and the cortical amygdala.

87 nctional coupling between OFC and olfactory (piriform) cortex and between vmPFC and amygdala revealed

88 ygdala, cingulate cortex, hippocampus (CA1), piriform cortex, and BNST were lower in OVX+E2 females c

89 us at 60 and 120 min following KA and in the piriform cortex, and central nucleus of the amygdala at

90 res were also observed in stratum oriens and piriform cortex, and in cerebellar Purkinje cell areas.

91 the precise laminar order of those from the piriform cortex, and provide a heavy caudal to rostral p

92 bral cortex, (predominantly in layer V), the piriform cortex, and the hippocampus (areas CA1, CA3 and

93 d with within-category pattern separation in piriform cortex, and the magnitude of this drug-induced

94 ry areas, the anterior olfactory nucleus and piriform cortex, and the olfactory associated orbital an

95 of the forebrain, including medial amygdala, piriform cortex, and ventrolateral septum, showed low c-

96 ; 4) olfactory-associated structures and the piriform cortex; and 5) sensory and motor trigeminal nuc

97 dal cell connections across the rat anterior piriform cortex (aPC) and found a pronounced gradient of

98 Ensemble activity patterns in anterior piriform cortex (APC) and orbitofrontal cortex (OFC) ref

99 P(+)) cells within the CC, Ctx, and anterior piriform cortex (aPC) and used prelabeling with 5-ethyny

100 Cells in the brain's anterior piriform cortex (APC) are sensitive to IAA deficiency, s

101 Layer 2 principal neurons in the anterior piriform cortex (APC) can be divided into 2 subtypes: se

102 The anterior piriform cortex (APC) has been shown to be an essential

103 NMDA receptor (NMDAR) number in the anterior piriform cortex (aPC) in rat induced by a 10 min pairing

104 he first time that adrenoceptors in anterior piriform cortex (aPC) must be engaged for adult rats to

105 ded neural ensemble activity in the anterior piriform cortex (aPC) of rats performing an odor mixture

106 rivation is in the highly excitable anterior piriform cortex (APC) of the brain.

107 ABA(A) and GABA(B) receptors in the anterior piriform cortex (APC) on intake of an amino acid imbalan

108 examines synaptic plasticity in the anterior piriform cortex (aPC) using ex vivo slices from rat pups

109 ction to the ventral portion of the anterior piriform cortex (APC) was substantial, while the dorsal

110 AA (DLAA) concentrations within the anterior piriform cortex (APC), and to a recognition process that

111 f IAA deficiency requires an intact anterior piriform cortex (APC), but does it act alone?

112 eurons in a small region within the anterior piriform cortex (aPC), termed the area tempestas (AT), r

113 ietary limiting amino (DLAA) in the anterior piriform cortex (APC).

114 specific odorant features, but the anterior piriform cortex (aPCX) and posterior piriform cortex (pP

115 striction, we hypothesized that the anterior piriform cortex (APCx) and the olfactory tubercle (OTu)

116 ral olfactory tract (LOT) fibers in anterior piriform cortex (aPCX) Layer Ia, Timm staining of associ

117 Anterior piriform cortex (aPCX) neurons rapidly filter repetitive

118 tized and recordings were made from anterior piriform cortex (aPCX).

119 w that spatial ensemble activity patterns in piriform cortex are closely linked to the perceptual mea

120 rceptual codes of odour quality in posterior piriform cortex are degraded in patients with Alzheimer'

121 The orbitofrontal cortex (OFC) and piriform cortex are involved in encoding the predictive

122 rocessing, the projections to the olfactory (piriform) cortex are more diffuse and show characteristi

123 cal application of bicuculline into anterior piriform cortex (area tempestas).

124 ocation to the physiologically defined "deep piriform cortex" ("area tempestas") from which convulsan

125 sured neural responses in primary olfactory (piriform) cortex as subjects smelled pairs of odorants s

126 hat the diversity in basket cell form in the piriform cortex, as in other areas of the cerebral corte

127 In contrast, in the piriform cortex, as in the majority of cortical regions,

128 KCC3a in the hippocampus, choroid plexus and piriform cortex, as well as KCC4 in the choroid plexus a

129 Primary olfactory (piriform) cortex, as well as anterior hippocampus, was a

130 on a large number (>1000) of other cells in piriform cortex at disparate locations.

131 lly to reach the ventral pallium deep to the piriform cortex at E14.5 in the mouse.

132 patial order in the bulb is discarded in the piriform cortex; axons from individual glomeruli project

133 ion-invariant neurons are overrepresented in piriform cortex but not in olfactory bulb mitral and tuf

134 gions, such as the hippocampus, thalamus, or piriform cortex, but not in the cerebellum beginning at

135 dy further explored LEC feedback to anterior piriform cortex by examining how LEC top-down input modu

136 bitrarily chosen subpopulation of neurons in piriform cortex can elicit different behavioral response

137 Steady-state interhemispheric anterior piriform cortex coherence is reduced during the initial

138 reduced microgliosis in the hippocampus and piriform cortex compared with T2(+/+)PS mice.

139 s have unique and redundant functions in the piriform cortex, controlling the timing of differentiati

140 e laminin immunoreactivity is present in the piriform cortex, corpus callosum (myelinated tracts) amy

141 ) and OT knock-out mouse in olfactory bulbs, piriform cortex, cortical amygdala, and the lateral sept

142 In piriform cortex, CRF1 binding increased in females and d

143 or representations in the primary olfactory (piriform) cortex depend on excitatory sensory afferents

144 al stimuli to sensory representations in the piriform cortex during odor-driven social learning.

145 glutamatergic pacemaker circuits within the piriform cortex, each of which can initiate waves of act

146 ons receiving primary olfactory projections (piriform cortex, entorhinal cortex, and amygdala).

147 to most basal forebrain areas including the piriform cortex, entorhinal cortex, insular cortex, orbi

148 We now report that OPCs in adult murine piriform cortex express low levels of doublecortin, a ma

149 ted olfactory epithelium and OB, but not the piriform cortex, express similar, sustained circadian rh

150 evated baseline, spontaneous activity in the piriform cortex extends the dynamic range of odor repres

151 e ipsilateral and contralateral OB, AON, and piriform cortex, few studies have examined this circuitr

152 hat extend, largely undiminished, across the piriform cortex, forming a large excitatory network that

153 Together these findings suggest that human piriform cortex has access to olfactory content in the t

154 Cholinergic modulation within the piriform cortex has long been proposed to serve importan

155 To determine whether OPCs in the piriform cortex have inherently different physiological

156 a tecta, and anterior olfactory tubercle and piriform cortex) have cells that express either calbindi

157 he highest level of labeling was seen in the piriform cortex, hippocampus, and thalamus.

158 n of high-affinity Epb sites was seen in the piriform cortex, hippocampus, caudate/putamen, and cereb

159 In rats and birds, the anterior piriform cortex houses the detector, but its mechanism h

160 ry formed between the olfactory bulb and the piriform cortex in anesthetized mice.

161 In recordings from anterior piriform cortex in awake behaving mice, we found that ne

162 PEA enhanced CBF in lateral frontal and piriform cortex in both KO and WILD mice.

163 ur study suggests a causal role of posterior piriform cortex in differentiating olfactory objects.

164 nd olfactory-related oscillations within the piriform cortex in vivo.

165 icited cross-adapting responses in posterior piriform cortex, in accord with the pattern observed in

166 revious reports, these findings suggest that piriform cortex includes multiple subdivisions, which ma

167 In the piriform cortex (including the endopiriform nucleus) of

168 Inactivation of piriform cortex increased odor responsiveness and pairwi

169 In the piriform cortex, individual odorants activate a unique e

170 s including the olfactory nuclei, neocortex, piriform cortex, induseum griseum, hippocampus, thalamus

171 assium changes demonstrates that SLEs in the piriform cortex initiate in the superficial layer 1 lack

172 Pyramidal cells in piriform cortex integrate sensory information from multi

173 Finally, post-training disruption of piriform cortex intracortical association fiber synapses

174 An interesting finding is the absence of the piriform cortex involvement in young male rats and the c

175 or layers I/II and layer III of the anterior piriform cortex ipsilateral and contralateral to the man

176 transsynaptic death of pyramidal neurons in piriform cortex is a nitric oxide-mediated event signale

177 gamma oscillations in the vStr LFP and that piriform cortex is an important driver of gamma-band osc

178 trated that a reduction in plasticity in the piriform cortex is associated with a selective impairmen

179 cells across major cortical subdivisions of piriform cortex is lacking.

180 These observations demonstrate that the piriform cortex is sufficient to elicit learned behavior

181 The olfactory (piriform) cortex is thought to generate odour percepts a

182 d, odor-distinctive patterns of responses in piriform cortex layer 2 principal cells: Approximately 1

183 tricted to the following D1+ CNS regions-the piriform cortex layer II, layers II-III of somatosensory

184 the peculiar organization of the superficial piriform cortex layers, which are characterized by unmye

185 Both right and left piriform cortex local field potential activities were re

186 ammed spatial relationships may not exist in piriform cortex, making flexible random associations the

187 oligodendrocytes (OLs), whereas those in the piriform cortex may also generate neurons.

188 activity during slow-wave states within the piriform cortex may be shaped by recent olfactory experi

189 learning until mastery, suggesting that each piriform cortex may contribute something unique to odour

190 ssion is seen in anterior olfactory nucleus, piriform cortex, median preoptic nucleus, basolateral am

191 The neural circuits of the piriform cortex mediate field potential oscillations and

192 In temporal piriform cortex, neural responses were evoked by the avC

193 cell fate and later to specify layer II/III piriform cortex neuronal identities.

194 We found that the overall spike rates of piriform cortex neurons (PCNs) were sensitive to the rel

195 Piriform cortex neurons from E14.5 mutant embryos displa

196 n a spatially scattered ensemble of anterior piriform cortex neurons, and the ensemble activity inclu

197 ng how LEC top-down input modulates anterior piriform cortex odor evoked activity in rats.

198 robust odor representations in the anterior piriform cortex of adult rats when odor was associated w

199 However, neurotoxicity in the piriform cortex of immature females treated for 60days a

200 gs of layer III non-pyramidal neurons in the piriform cortex of Sprague-Dawley rats.

201 thelium, main olfactory bulb, and olfactory (piriform) cortex of CNGA2 knock-out mice.

202 sensory paleocortex, the primary olfactory (piriform) cortex of mice.

203 might participate in seizure circuitry: the piriform cortex, olfactory tubercle, nucleus accumbens,

204 sensory input in the olfactory bulb through piriform cortex/olfactory bulb synaptic interactions.

205 educes olfactory bulb afferent excitation of piriform cortex, on apoptosis (terminal deoxynucleotidyl

206 tive cell numbers were high in, for example, piriform cortex, paraventricular nucleus, supraoptic nuc

207 tion, the analysis of neural circuits in the piriform cortex (PC) demonstrated the importance of not

208 ng from the association fiber (AF) system in piriform cortex (PC) make axodendritic synapses on granu

209 inhibitory and glutamatergic neurons in the piriform cortex (PC) of mice.

210 nic synapses (AASs) in brain slices from the piriform cortex (PC) of mice.

211 n adult rat olfactory bulb (OB) and anterior piriform cortex (PC) were assessed after discrimination

212 For the piriform cortex (PC), results with this technique indica

213 nts (PLC) in potentials evoked in the OB and piriform cortex (PC), while leaving the monosynaptic EPS

214 ation of cortical association fibers (AF) in piriform cortex (PC).

215 these mitral/tufted cells in turn project to piriform cortex (PC).

216 ral and granular layers of the OB and in the piriform cortex (PC).

217 ct regions: olfactory bulb (OB) and anterior piriform cortex (PC).

218 and polysynaptically) to primary olfactory (piriform) cortex (PC)-connections that might be hypothes

219 Hyperactive odor-evoked activity in the piriform cortex (PCX) and increased OB-PCX functional co

220 s, we found that 26% of neurons in the mouse piriform cortex (PCX) display modulation in firing to ca

221 The piriform cortex (PCX) is the largest component of the ol

222 s well as local field potentials in the MDT, piriform cortex (PCX), and OFC in rats performing a two-

223 In the piriform cortex (PCx), spatially dispersed sensory input

224 electrophysiological recordings in anterior piriform cortex (PCx), we assessed how cortical neurons

225 Our results suggest that piriform cortex performs correlative functions analogous

226 nigra (VTA/SN), nucleus accumbens (NAc), and piriform cortex (PFx)-after bilateral olfactory bulbecto

227 rapid elevation of CRH concentrations at the piriform cortex (Pir) and hypothalamic nuclei following

228 neurodegeneration were seen in the posterior piriform cortex (Pir), posteriolateral cortical amygdalo

229 ions, a frontal subregion comprising frontal piriform cortex (PirF) and the olfactory tubercle respon

230 eas a temporal subregion comprising temporal piriform cortex (PirT) responded equally across conditio

231 e-associated astrocytes" (SAAs) in posterior piriform cortex (PPC) are unique by virtue of a direct a

232 ributed ensemble activity in human posterior piriform cortex (PPC) coincides with perceptual ratings

233 resentations of the odor target in posterior piriform cortex (PPC) gave way to poststimulus represent

234 Retrograde tracing from the OB or posterior piriform cortex (PPC) showed that the APC projects to th

235 ons positive for GAD65-EGFP in the posterior piriform cortex (PPC).

236 from single neurons in posterior olfactory (piriform) cortex (pPC) of awake rats while presenting ba

237 nterior piriform cortex (aPCX) and posterior piriform cortex (pPCX) differ markedly in their anatomic

238 The piriform cortex provides an ideal system to address this

239 However, piriform cortex pyramidal cells also receive dense intra

240 espread and broadly tuned than excitation in piriform cortex pyramidal cells.

241 enhanced intrinsic neuronal excitability of piriform cortex pyramidal neurons, and in their excitato

242 are primarily located in the in the adjacent piriform cortex rather than in the vStr itself, providin

243 ve suggested a model in which neurons of the piriform cortex receive convergent input from random col

244 n to provide direct evidence that neurons in piriform cortex receive convergent synaptic input from d

245 The olfactory bulb (OB) and piriform cortex receive dense cholinergic projections fr

246 to the olfactory bulb, such that concurrent piriform cortex recordings show no evidence of enhanced

247 d to all odors, whereas activity in anterior piriform cortex reflected sensitivity to odor affect.

248 lt CNS-though rare, neuron production in the piriform cortex remains a possibility.

249 Neurons in piriform cortex, responsive to a given odorant, are not

250 es the composition of synaptic NMDARs in the piriform cortex, resulting in receptors with a higher co

251 ves dorsal olfactory bulb input, whereas the piriform cortex samples the whole olfactory bulb without

252 ocally; and (6) the endopiriform nucleus and piriform cortex share target areas, but efferents from t

253 DCX and PSA-NCAM immunoreactive cells in the piriform cortex, similar to that previously reported in

254 Here we used patch-clamp recordings in rat piriform cortex slices to examine cellular mechanisms th

255 In primary olfactory (piriform) cortex, spatially and temporally dissociable r

256 cus on the hippocampus, somatosensory, paleo/piriform cortex, striatum, and various amygdala nuclei.

257 ositive, we showed that in the motor cortex, piriform cortex, striatum, CA1 region of the hippocampus

258 , known to abolish gamma oscillations in the piriform cortex, strongly reduced vStr gamma power and t

259 the c-Fos protein has been evidenced in the piriform cortex, subiculum, entorhinal and perirhinal co

260 mmunoreactivity were found in the claustrum, piriform cortex (superficial layer), arcuate hypothalami

261 nigra, but was increased bilaterally in the piriform cortex, supraoptic nucleus, central nucleus of

262 onic synapse are significantly higher in the piriform cortex than in the neocortex.

263 a population of neurons within the anterior piriform cortex that undergo rapid apoptosis following d

264 The anterior part of the piriform cortex (the APC) has been the focus of cortical

265 However, in piriform cortex, the activity of target neurons increase

266 The AC is composed of axons from the piriform cortex, the anterior olfactory nucleus and the

267 idual recognition, particularly the anterior piriform cortex, the CA1 and CA3 regions of anterior dor

268 riched for oxytocin receptors, including the piriform cortex, the left auditory cortex, and CA2 of th

269 a significant projection to OFC arises from piriform cortex, the traditional primary olfactory corte

270 Within piriform cortex these arbors are highly distributed with

271 achnoid (> or =3 hours), particularly within piriform cortex; this activity was suppressed by injecti

272 tiple relays in a network extending from the piriform cortex through the hippocampus can be different

273 fMRI data for a node within the ipsilateral piriform cortex to be important for seizure modulation i

274 We introduced channelrhodopsin into the piriform cortex to characterize these intrinsic circuits

275 dendrites and that feedback projections from piriform cortex to olfactory bulb interneurons are a sou

276 stablished major neural pathways linking the piriform cortex to other cortical and subcortical region

277 aired single-unit recordings in rat anterior piriform cortex to test several predictions regarding en

278 heavy, rather selective projection from the piriform cortex to the ventrolateral orbital cortex (VLO

279 orsal (MD) thalamus links primary olfactory (piriform) cortex to olfactory neocortical projection sit

280 revious work showing that pyramidal cells in piriform cortex undergo classical apoptosis within 24 h

281 d by theta burst stimulation in the anterior piriform cortex was normal in KO mice aged < 6 months bu

282 Notably, the projection to piriform cortex was predominantly from ventrolateral orb

283 A nonhabituating response in posterior piriform cortex was tuned to all odors, whereas activity

284 hereas cingulate cortex and to a less extent piriform cortex were affected preferentially by the CIV

285 gs from both the olfactory bulb and anterior piriform cortex were performed in freely breathing ureth

286 DCX and PSA-NCAM immunoreactive cells in the piriform cortex were quantified as measures of plasticit

287 put/output curves for two connections in the piriform cortex were similar to those for the LPP, where

288 Odor representations in anterior piriform cortex were sparser than typical in adult rat a

289 nections of pyramidal cells in rat posterior piriform cortex were studied by direct visualization of

290 I-III of the parietal cortex and superficial piriform cortex were the most sensitive followed by othe

291 ing channelrhodopsin at multiple loci in the piriform cortex, when paired with reward or shock, elici

292 tern does not appear to be maintained in the piriform cortex, where stimuli appear to be coded in a d

293 ur results indicate a double dissociation in piriform cortex, whereby posterior regions encode qualit

294 nt mice presented a reduced thickness of the piriform cortex, which affected projection neurons in la

295 enerated in the forebrain, especially in the piriform cortex, which is the main target of the olfacto

296 here is a population of superficial cells in piriform cortex whose survival is tightly regulated by s

297 ity of the olfactory cortex, principally the piriform cortex, will be described in the context of how

298 ical loop between the olfactory bulb and the piriform cortex, with cortex explaining incoming activit

299 or stimulation enhanced theta power in human piriform cortex, with robust effects at the level of sin

300 o-active neurons that are distributed across piriform cortex without any apparent spatial organizatio